Canonical Allele Identifier: CA1156102303
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2078164442
gnomAD v4: 1-17054022-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17054022T>C , CM000663.2:g.17054022T>C GRCh38
NC_000001.10:g.17380517T>C , CM000663.1:g.17380517T>C GRCh37
NC_000001.9:g.17253104T>C NCBI36
NG_012340.1:g.5149A>G , LRG_316:g.5149A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375499.8:c.-3A>G MANE Select ENSP00000364649.3:n.-3A>G
ENST00000375499.7:c.-3A>G ENSP00000364649.3:n.-3A>G
ENST00000466613.2:n.10A>G
NM_003000.2:c.-3A>G , LRG_316t1:c.-3A>G NP_002991.2:n.-3A>G
NM_003000.3:c.-3A>G MANE Select NP_002991.2:n.-3A>G